Highly diastereoselective Claisen rearrangement leading to vicinal quaternary carbons construction of oxindoles-Reference-Cited by-同舟云学术

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Highly diastereoselective Claisen rearrangement leading to vicinal quaternary carbons construction of oxindoles

Published:2011-11 Issue:46 Volume:52 Page:6199-6202
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Matsuta Yumiko,Kobari Takayuki,Kurashima Sachiko,Kumakura Yuhsuke,Shinada Masashi,Higuchi Kazuhiro,Kawasaki Tomomi

Funder

Grants-in-Aid for Scientific Research

High-Tech Research Center Project

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference49 articles.

1. Stereoselective formation of quaternary carbon centers and related functions

2. Asymmetric Catalysis Special Feature Part I: Catalytic asymmetric synthesis of all-carbon quaternary stereocenters

3. Contiguous stereogenic quaternary carbons: A daunting challenge in natural products synthesis

4. Catalytic Enantioselective Construction of All-Carbon Quaternary Stereocenters

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. [3,3]-Sigmatropic rearrangements: a variety of methods and recent advances;Russian Chemical Reviews;2022

2. A concise approach for central core of trigolutes: Total synthesis of trigolute B and 3- epi -trigolute B and analogues;Tetrahedron;2017-02

3. Cascade synthesis of spirooxindole δ-lactone derivatives through N-aryl hydroxymethylacrylamides with xanthates;Tetrahedron;2015-10

4. Direct construction of vicinal all-carbon quaternary stereocenters in natural product synthesis;Natural Product Reports;2015

5. Recent Developments on the Synthesis and Applications of Natural Products-Inspired Spirooxindole Frameworks;Studies in Natural Products Chemistry;2015

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